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1 ophan binding now allows the formation of an occluded state.
2 rity-dependent structural transitions to the occluded state.
3 ho84 from an open, inward-facing state to an occluded state.
4 site from an outwardly to an inwardly facing occluded state.
5 s of Bor1 have rotated inwards to achieve an occluded state.
6 les of E. coli confirmed the presence of the occluded state.
7 ic conformations, yielding an outward-facing occluded state.
8 y described structures in outward-facing and occluded states.
9 rmational transitions between the closed and occluded states.
10 to promote the structural transition to the occluded state, a step in the transport cycle that is de
11 ubstrate binding and in the formation of the occluded state and to investigate the dynamics of this s
12 binding site to generate a substrate-bound, occluded state, and non-conservative mutation of Tyr130
13 y HDX patterns, revealing that the ion-bound/occluded states are much more stable (rigid) in the OF t
14 substrate appears to stabilize the partially occluded state, as in the two apo simulations either no
15 to 3.6 A resolution, reveals a ligand-bound occluded state for the MFS and provides new insights int
16 formation indicates that a water-impermeable occluded state (glucose and Na(+) in their binding pocke
17 (Aa), a prokaryotic NSS homolog, revealed an occluded state in which one leucine and two Na(+) ions a
18 ne in an apparently open state and one in an occluded state, indicating that SemiSWEETs and SWEETs ar
21 an extracellular gate that closes to form an occluded state is strongly supported by conformational s
23 molecular dynamics (MD) trajectories of the occluded state of the bacterial leucine transporter LeuT
24 r dynamic simulation showed that a sustained occluded state of the transporter upon binding to co-tra
26 galactopyranosides specifically, inducing an occluded state that can open to either side of the membr
27 es transitions between a closed state and an occluded state via an intermediate "open" conformation.
28 e course of MD simulations starting from the occluded state with bound Na(+), but in the absence of s
29 ward-open character and is lower than in the occluded state with bound substrate; however, the Na1 si
31 phate transporter, PiPT, in an inward-facing occluded state, with bound phosphate visible in the memb
32 lodurans, have been resolved in novel inward-occluded states, with the extracellular vestibule closed
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